PACEMAKER, ANTRIO-VENTRICULAR SEQ.

PACEMAKER, ANTRIO-VENTRICULAR SEQ. is an FDA 510(k)-cleared medical device (K770328) manufactured by American Pacemaker Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on February 27, 1977. Regulation: 8.